Canonical Allele Identifier: CA1397109291

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120674936C= , CM000665.2:g.120674936C=	GRCh38
NC_000003.11:g.120393783C= , CM000665.1:g.120393783C=	GRCh37
NC_000003.10:g.121876473C=	NCBI36
NG_011957.1:g.12546G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.141G= MANE Select	ENSP00000283871.5:p.Ser47=
ENST00000283871.9:c.141G=	ENSP00000283871.5:p.Ser47=
ENST00000466528.5:n.167G=
ENST00000476082.2:c.53+856G=	ENSP00000419560.2:n.53+856G=
ENST00000480862.1:n.299G=
ENST00000485313.5:n.249G=
ENST00000488183.5:n.399G=
NM_000187.3:c.141G=	NP_000178.2:p.Ser47=
XM_005247412.1:c.141G=	XP_005247469.1:p.Ser47=
XM_005247413.1:c.141G=	XP_005247470.1:p.Ser47=
XM_005247414.3:c.141G=	XP_005247471.1:p.Ser47=
XM_011512746.1:c.141G=	XP_011511048.1:p.Ser47=
XM_005247412.2:c.141G=	XP_005247469.1:p.Ser47=
XM_005247413.2:c.141G=	XP_005247470.1:p.Ser47=
XM_005247414.5:c.141G=	XP_005247471.1:p.Ser47=
XM_011512746.2:c.141G=	XP_011511048.1:p.Ser47=
XM_017006277.2:c.-283G=	XP_016861766.1:n.-283G=
NM_000187.4:c.141G= MANE Select	NP_000178.2:p.Ser47=